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1,2,3,4,5,6,7,8-OCTAPROPYLANTHRACENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

358753-30-7

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358753-30-7 Usage

Chemical class

Polycyclic aromatic hydrocarbons (PAHs)

Derived from

Anthracene, a three-ringed aromatic hydrocarbon

Structure

Eight propyl groups attached to the carbon atoms of the anthracene molecule

Common uses

a. Precursor in the synthesis of organic materials
b. Production of various industrial products
c. Organic electronic devices (OLEDs, organic solar cells, and organic field-effect transistors)

Environmental impact

Considered an environmental pollutant

Health hazards

Potential human health hazard due to carcinogenic and mutagenic properties

Regulatory considerations

Use and handling should be carefully regulated to minimize exposure risks

Check Digit Verification of cas no

The CAS Registry Mumber 358753-30-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,8,7,5 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 358753-30:
(8*3)+(7*5)+(6*8)+(5*7)+(4*5)+(3*3)+(2*3)+(1*0)=177
177 % 10 = 7
So 358753-30-7 is a valid CAS Registry Number.

358753-30-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,5,6,7,8-octapropylanthracene

1.2 Other means of identification

Product number -
Other names Anthracene,1,2,3,4,5,6,7,8-octapropyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:358753-30-7 SDS

358753-30-7Downstream Products

358753-30-7Relevant articles and documents

Pd-catalyzed reactions of o-diiodoarenes with alkynes for aromatic ring extension

Huang, Wenying,Zhou, Xin,Kanno, Ken-Ichiro,Takahashi, Tamotsu

, p. 2429 - 2431 (2004)

(Equation Presented) A new and efficient palladium-catalyzed reaction of o-diiodoarenes with internal alkynes produces naphthalenes or anthracenes in good to excellent yields. This procedure provides a simple, catalytic, and straightforward ring-extension method for constructing substituted polycyclic aromatic compounds.

Synthesis of acenes via coupling of 1,4-dilithiobutadienes with diiodoarenes in the presence of CuCl

Zhou, Lishan,Nakajima, Kiyohiko,Kanno, Ken-ichiro,Takahashi, Tamotsu

supporting information; experimental part, p. 2722 - 2726 (2009/09/06)

Dilithiobutadienes prepared from diiodobutadienes reacted with diiodobenzene or diiodonaphthalene to afford substituted naphthalene, anthracene, dihydronaphthacene, and dihydropentacene derivatives in the presence of CuCl and DMPU. Dihydronaphthacene and

Polyacene derivatives and production thereof

-

, (2008/06/13)

The present invention relates to polyacene derivatives represented by general formula (I) below: (wherein R1 to R10, etc. each represents hydrogen atom, hydrocarbon group, or an alkoxy group; A1 and A2 are hydro

Aromatization of highly alkyl-substituted dihydroanthracenes using n-BuLi/TMEDA/MeI

Kitamura, Masanori,Shen, Baojian,Liu, Yanjun,Zheng, Hegen,Takahashi, Tamotsu

, p. 646 - 647 (2007/10/03)

Aromatization of highly alkyl-substituted dihydroanthracene was performed with the n-BuLi/TMEDA/MeI. Treatment of 1,2,3,4,5,6,7,8-octapropyl-9, 10-dihydroanthracene with 2.2 equiv of n-BuLi, TMEDA at 50 °C in hexane for 3 h, followed by 1.1 equiv of MeI at room temperature for 1 h gave the corresponding anthracene in 98% yield.

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